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The Journal of Clinical Endocrinology and Metabolism|November 2, 2006
Sodium/iodide symporter (NIS) gene expression is the limiting step for the onset of thyroid function in the human fetusGabor Szinnai, Ludovic Lacroix, Aurore Carré, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 26, 2014
Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portionTaise Lima Oliveira Cerqueira, Aurore Carré, Lucie Chevrier, et al.
Ebiomedicine|October 13, 2016
CACNA1H Mutations Are Associated With Different Forms of Primary AldosteronismGeorgios Daniil, Fabio L Fernandes-Rosa, Jean Chemin, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2004
Incidence of growth hormone deficiency in pediatric-onset Langerhans cell histiocytosis: efficacy and safety of growth hormone treatmentJean Donadieu, Maria-Alejandra Rolon, Isabelle Pion, et al.
Hormone Research in Paediatrics|April 11, 2012
Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndromeRaphaël Teissier, Loïc Guillot, Aurore Carré, et al.
Journal of Neurosurgery. Pediatrics|August 4, 2009
Hypothalamic lipoma associated with severe obesity. Report of 2 casesStéphanie Puget, Matthew R Garnett, Delphine Leclercq, et al.
JIMD Reports|March 6, 2023
Early treatment of neonatal diabetes with oral glibenclamide in an extremely preterm infantAlfonso Galderisi, Elsa Kermorvant-Duchemin, Alejandra Daruich, et al.
Cell Metabolism|May 3, 2016
Age-Dependent Pancreatic Gene Regulation Reveals Mechanisms Governing Human β Cell FunctionH Efsun Arda, Lingyu Li, Jennifer Tsai, et al.
Journal of the Endocrine Society|November 13, 2025
Adherence and Growth Outcomes in a Large Cohort of Children Treated With Recombinant GH Using a Connected Auto-injectorMichel Polak, Natacha Bouhours-Nouet, Paula van Dommelen, et al.
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